Canonical Allele Identifier: CA2418091386

Gene: PHKA2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18950915A= , CM000685.2:g.18950915A=	GRCh38
NC_000023.10:g.18969033A= , CM000685.1:g.18969033A=	GRCh37
NC_000023.9:g.18878954A=	NCBI36
NG_016622.1:g.38448T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379942.5:c.454+189T= MANE Select	ENSP00000369274.4:n.454+189T=
ENST00000379942.4:c.454+189T=	ENSP00000369274.4:n.454+189T=
NM_000292.2:c.454+189T=	NP_000283.1:n.454+189T=
XM_005274548.3:c.454+189T=	XP_005274605.1:n.454+189T=
XM_005274550.3:c.454+189T=	XP_005274607.1:n.454+189T=
XM_006724496.2:c.454+189T=	XP_006724559.1:n.454+189T=
XM_006724498.2:c.-93+1579T=	XP_006724561.1:n.-93+1579T=
XM_011545537.1:c.454+189T=	XP_011543839.1:n.454+189T=
XR_950461.1:n.638+189T=
XM_005274548.5:c.454+189T=	XP_005274605.1:n.454+189T=
XM_005274550.5:c.454+189T=	XP_005274607.1:n.454+189T=
XM_006724496.4:c.454+189T=	XP_006724559.1:n.454+189T=
XM_006724498.4:c.-93+1579T=	XP_006724561.1:n.-93+1579T=
XM_011545537.3:c.454+189T=	XP_011543839.1:n.454+189T=
XM_017029580.2:c.-388+189T=	XP_016885069.1:n.-388+189T=
XR_001755697.2:n.624+189T=
XR_001755698.2:n.624+189T=
XR_002958777.1:n.624+189T=
XR_950461.3:n.624+189T=
NM_000292.3:c.454+189T= MANE Select	NP_000283.1:n.454+189T=